Incidental Mutation 'IGL01795:4930451G09Rik'
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ID155328
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930451G09Rik
Ensembl Gene ENSMUSG00000022543
Gene NameRIKEN cDNA 4930451G09 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.080) question?
Stock #IGL01795
Quality Score
Status
Chromosome16
Chromosomal Location4968936-4978962 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to G at 4974071 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000090457]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000090457
SMART Domains Protein: ENSMUSP00000087942
Gene: ENSMUSG00000022543

DomainStartEndE-ValueType
Pfam:DUF4701 1 195 7.5e-72 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229669
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930572O03Rik C A 5: 15,656,886 probably benign Het
4930590J08Rik C T 6: 91,918,112 R263* probably null Het
Arfgef1 A T 1: 10,147,528 I1562K probably benign Het
B4galt1 T A 4: 40,807,760 D347V probably damaging Het
Ccdc178 T A 18: 22,019,118 R646S probably benign Het
Ccr1 A T 9: 123,964,112 L127* probably null Het
Cd109 A G 9: 78,661,765 probably benign Het
Chd6 A G 2: 160,961,374 V2128A probably benign Het
Chil6 T A 3: 106,388,792 I376F probably damaging Het
Chit1 T C 1: 134,148,429 S275P probably damaging Het
Erap1 T A 13: 74,666,090 probably null Het
F5 T C 1: 164,194,390 V1478A probably benign Het
Fras1 G T 5: 96,778,045 V3703F probably damaging Het
Hmmr C T 11: 40,721,734 M185I probably benign Het
Kcnu1 A G 8: 25,913,705 Y8C probably damaging Het
Krt16 A G 11: 100,247,724 probably benign Het
Mcf2l A G 8: 13,000,749 probably null Het
Mgat5 C T 1: 127,469,231 R572W probably damaging Het
Neil2 T C 14: 63,188,750 D57G probably benign Het
Nom1 A G 5: 29,446,871 T736A probably benign Het
Olfr1030 T A 2: 85,984,134 I98N probably damaging Het
Olfr1301 A T 2: 111,754,386 M46L probably benign Het
Olfr414 A T 1: 174,430,649 I74F possibly damaging Het
Prr14l A T 5: 32,831,845 probably benign Het
Sall1 A G 8: 89,028,680 S1224P probably benign Het
Slc44a2 A C 9: 21,345,349 K336Q probably damaging Het
Sptan1 C T 2: 30,018,489 T1754I probably benign Het
Zdhhc5 T C 2: 84,690,046 S596G probably benign Het
Other mutations in 4930451G09Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03052:4930451G09Rik APN 16 4977494 splice site noncoding transcript
R0392:4930451G09Rik UTSW 16 4977499 splice site noncoding transcript
R4851:4930451G09Rik UTSW 16 4976274 exon noncoding transcript
R5562:4930451G09Rik UTSW 16 4974076 exon noncoding transcript
R5868:4930451G09Rik UTSW 16 4974068 exon noncoding transcript
Posted On2014-02-04